Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2228243
rs2228243
HRG ; LOC105374258
3 1.000 0.080 3 186677324 missense variant A/G;T snv 0.20; 4.0E-06 0.700 1.000 1 2013 2013
dbSNP: rs6009
rs6009
F5
3 1.000 0.080 1 169529596 intron variant T/A;C snv 0.94 0.700 1.000 1 2013 2013
dbSNP: rs6427196
rs6427196
F5
3 1.000 0.080 1 169511985 3 prime UTR variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs6682179
rs6682179
F5
2 1.000 0.080 1 169521163 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs9898
rs9898
HRG ; LOC105374258
3 0.925 0.160 3 186672838 missense variant C/T snv 0.38 0.43 0.700 1.000 1 2013 2013